1-AZIRIDINECARBOXAMIDE, N-(p-NITROPHENYL)-

Base Information

Chemical Name:1-AZIRIDINECARBOXAMIDE, N-(p-NITROPHENYL)-
CAS No.:3647-22-1
Molecular Formula:C9H9N3O3
Molecular Weight:207.1861
Hs Code.:2933990090
DSSTox Substance ID:DTXSID00189980
Wikidata:Q83062217
Mol file:3647-22-1.mol

Synonyms:BRN 1346959;3647-22-1;1-AZIRIDINECARBOXAMIDE, N-(p-NITROPHENYL)-;1-(1-Aziridinyl)-N-(p-nitrophenyl)formamide;Formamide, 1-(1-aziridinyl)-N-(p-nitrophenyl)-;DTXSID00189980;1-Aziridinecarboxanilide, 4'-nitro-;LS-23226

Suppliers and Price of 1-AZIRIDINECARBOXAMIDE, N-(p-NITROPHENYL)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of 1-AZIRIDINECARBOXAMIDE, N-(p-NITROPHENYL)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：77.93000
Density:1.537g/cm³
LogP:1.97640
XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:207.06439116
Heavy Atom Count:15
Complexity:264

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN1C(=O)NC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of 1-AZIRIDINECARBOXAMIDE, N-(p-NITROPHENYL)-

There total 1 articles about 1-AZIRIDINECARBOXAMIDE, N-(p-NITROPHENYL)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 3647-22-1
aziridine-1-carboxylic acid 4-nitro-anilide

Guidance literature:: Ethylenimin, 4-Nitro-phenylisocyanat, Diethylether;

Reference yield:

: 3647-22-1
aziridine-1-carboxylic acid 4-nitro-anilide

: C₉H₁₁N₅O₅

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / 2 h / 50 °C

2: NH₃ / CH₂Cl₂ / cooling

With ammonia; In ethanol; dichloromethane;
DOI:10.3797/scipharm.aut-01-13